{
  "id": 23812,
  "label": "congenital/infantile spindle cell rhabdomyosarcoma with VGLL2/NCOA2/CITED2 rearrangements",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0100060",
  "properties": {
    "xrefs": [
      "GARD:0026030",
      "MEDGEN:1791325",
      "NCIT:C178232",
      "UMLS:C5554884"
    ],
    "definition": "Congenital/infantile spindle cell rhabdomyosarcoma characterized by the presence of gene fusions involving the VGLL2, SRF, TEAD1, NCOA2, and CITED2 genes."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 4642,
      "label": "spindle cell rhabdomyosarcoma",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4933,
        6928
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:3260",
          "GARD:0023175",
          "ICD9:171.9",
          "ICDO:8912/3",
          "MEDGEN:224766",
          "NCIT:C6519",
          "ONCOTREE:SCRMS",
          "SCTID:404055006",
          "UMLS:C1266134"
        ],
        "synonyms": [
          "spindle cell rhabdomyosarcoma (morphologic abnormality)",
          "SCRMS"
        ],
        "definition": "An uncommon variant of rhabdomyosarcoma characterized by the presence of whorls of spindle cells forming a storiform pattern. In children it usually arises in the paratesticular region. In adults it usually arises from the deep soft tissues in the head and neck."
      },
      "child_count": 6,
      "reference_id": "MONDO:0002581"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 4642,
      "label": "spindle cell rhabdomyosarcoma"
    }
  ]
}